Canonical Allele Identifier: CA3576009
Gene: FGFR4 HGNC NCBI

Linked Data

dbSNP Id: rs745405031

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177090896_177090897insAAGA , CM000667.2:g.177090896_177090897insAAGA GRCh38
NC_000005.9:g.176517897_176517898insAAGA , CM000667.1:g.176517897_176517898insAAGA GRCh37
NC_000005.8:g.176450503_176450504insAAGA NCBI36
NG_012067.1:g.8977_8978insAAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000292408.9:c.437-42_437-41insAAGA MANE Select ENSP00000292408.4:n.437-42_437-41insAAGA
ENST00000292408.8:c.437-42_437-41insAAGA ENSP00000292408.4:n.437-42_437-41insAAGA
ENST00000393637.5:c.437-42_437-41insAAGA ENSP00000377254.1:n.437-42_437-41insAAGA
ENST00000393648.6:c.437-42_437-41insAAGA ENSP00000377259.2:n.437-42_437-41insAAGA
ENST00000426612.5:n.512_513insAAGA
ENST00000430285.5:c.*301-42_*301-41insAAGA ENSP00000395164.1:n.*301-42_*301-41insAAGA
ENST00000502906.5:c.437-42_437-41insAAGA ENSP00000424960.1:n.437-42_437-41insAAGA
ENST00000503708.5:c.437-42_437-41insAAGA ENSP00000424905.1:n.437-42_437-41insAAGA
ENST00000509511.5:n.437-42_437-41insAAGA
NM_001291980.1:c.437-42_437-41insAAGA NP_001278909.1:n.437-42_437-41insAAGA
NM_002011.4:c.437-42_437-41insAAGA NP_002002.3:n.437-42_437-41insAAGA
NM_022963.3:c.437-42_437-41insAAGA NP_075252.2:n.437-42_437-41insAAGA
NM_213647.2:c.437-42_437-41insAAGA NP_998812.1:n.437-42_437-41insAAGA
XM_005265838.2:c.437-42_437-41insAAGA XP_005265895.1:n.437-42_437-41insAAGA
XM_011534464.1:c.530-42_530-41insAAGA XP_011532766.1:n.530-42_530-41insAAGA
XM_011534465.1:c.119-42_119-41insAAGA XP_011532767.1:n.119-42_119-41insAAGA
XR_941090.1:n.482-42_482-41insAAGA
NM_001354984.1:c.437-42_437-41insAAGA NP_001341913.1:n.437-42_437-41insAAGA
NM_213647.3:c.437-42_437-41insAAGA MANE Select NP_998812.1:n.437-42_437-41insAAGA
NM_001291980.2:c.437-42_437-41insAAGA NP_001278909.1:n.437-42_437-41insAAGA
NM_001354984.2:c.437-42_437-41insAAGA NP_001341913.1:n.437-42_437-41insAAGA
NM_002011.5:c.437-42_437-41insAAGA NP_002002.3:n.437-42_437-41insAAGA